Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes-Reference-Cited by-同舟云学术

Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes

Published:2009-10-18 Issue:1 Volume:10 Page:
ISSN:1471-2156
Container-title:BMC Genetics
language:en
Short-container-title:BMC Genet

Author:

Bennett Richard R,Schneider Hal E,Estrella Elicia,Burgess Stephanie,Cheng Andrew S,Barrett Caitlin,Lip Va,Lai Poh San,Shen Yiping,Wu Bai-Lin,Darras Basil T,Beggs Alan H,Kunkel Louis M

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2156-10-66.pdf

Reference34 articles.

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3. van Essen AJ, Busch HF, te Meerman GJ, ten Kate LP: Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands. Hum Genet. 1992, 88: 258-266.

4. Emery AE: Population frequencies of inherited neuromuscular diseases--a world survey. Neuromuscul Disord. 1991, 1: 19-29. 10.1016/0960-8966(91)90039-U.

5. Cowan J, Macdessi J, Stark A, Morgan G: Incidence of Duchenne muscular dystrophy in New South Wales and Australian Capital Territory. J Med Genet. 1980, 17: 245-249. 10.1136/jmg.17.4.245.

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